Details
| Original language | English |
|---|---|
| Pages (from-to) | 568-571 |
| Number of pages | 4 |
| Journal | Organic Letters |
| Volume | 16 |
| Issue number | 2 |
| Publication status | Published - 17 Jan 2014 |
Abstract
The antibiotic elansolid B1 was prepared by a convergent strategy that relied on a highly diastereoselective, biomimetic intramolecular Diels-Alder cycloaddition (IMDA) that furnished the tetrahydroindane unit. Other key features are a double Sonogashira cross-coupling and a substratecontrolled Yamamoto aldol reaction.
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)
- Biochemistry
- Chemistry(all)
- Physical and Theoretical Chemistry
- Chemistry(all)
- Organic Chemistry
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In: Organic Letters, Vol. 16, No. 2, 17.01.2014, p. 568-571.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Total synthesis of the antibiotic Elansolid B1
AU - Weber, Arne
AU - Dehn, Richard
AU - Schläger, Nadin
AU - Dieter, Bastian
AU - Kirschning, Andreas
N1 - Copyright: Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2014/1/17
Y1 - 2014/1/17
N2 - The antibiotic elansolid B1 was prepared by a convergent strategy that relied on a highly diastereoselective, biomimetic intramolecular Diels-Alder cycloaddition (IMDA) that furnished the tetrahydroindane unit. Other key features are a double Sonogashira cross-coupling and a substratecontrolled Yamamoto aldol reaction.
AB - The antibiotic elansolid B1 was prepared by a convergent strategy that relied on a highly diastereoselective, biomimetic intramolecular Diels-Alder cycloaddition (IMDA) that furnished the tetrahydroindane unit. Other key features are a double Sonogashira cross-coupling and a substratecontrolled Yamamoto aldol reaction.
UR - http://www.scopus.com/inward/record.url?scp=84896759510&partnerID=8YFLogxK
U2 - 10.1021/ol403441c
DO - 10.1021/ol403441c
M3 - Article
C2 - 24393030
AN - SCOPUS:84896759510
VL - 16
SP - 568
EP - 571
JO - Organic Letters
JF - Organic Letters
SN - 1523-7060
IS - 2
ER -